Disease: Congenital Abnormality ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality 		0.010 Biomarker group BEFREE These results also implicate genes encoding other TRK and neurotrophin family members as candidates for developmental defect(s) of the nervous system. 8696348 1996